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Apoptosis signal-regulating kinase 1 inhibition in in vivo and in vitro models of pulmonary hypertension.
Wilson, Kathryn S; Buist, Hanna; Suveizdyte, Kornelija; Liles, John T; Budas, Grant R; Hughes, Colin; MacLean, Margaret R; Johnson, Martin; Church, Alistair C; Peacock, Andrew J; Welsh, David J.
Affiliation
  • Wilson KS; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Buist H; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Suveizdyte K; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Liles JT; Gilead Sciences Inc., Foster City, CA, USA.
  • Budas GR; Gilead Sciences Inc., Foster City, CA, USA.
  • Hughes C; Central Research Facility, University of Glasgow, Glasgow, UK.
  • MacLean MR; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Johnson M; Scottish Pulmonary Vascular Unit, Golden Jubilee National Hospital, Clydebank, UK.
  • Church AC; Scottish Pulmonary Vascular Unit, Golden Jubilee National Hospital, Clydebank, UK.
  • Peacock AJ; Scottish Pulmonary Vascular Unit, Golden Jubilee National Hospital, Clydebank, UK.
  • Welsh DJ; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Pulm Circ ; 10(2): 2045894020922810, 2020.
Article in En | MEDLINE | ID: mdl-32523684
ABSTRACT
Pulmonary arterial hypertension, group 1 of the pulmonary hypertension disease family, involves pulmonary vascular remodelling, right ventricular dysfunction and cardiac failure. Oxidative stress, through activation of mitogen-activated protein kinases is implicated in these changes. Inhibition of apoptosis signal-regulating kinase 1, an apical mitogen-activated protein kinase, prevented pulmonary arterial hypertension developing in rodent models. Here, we investigate apoptosis signal-regulating kinase 1 in pulmonary arterial hypertension by examining the impact that its inhibition has on the molecular and cellular signalling in established disease. Apoptosis signal-regulating kinase 1 inhibition was investigated in in vivo pulmonary arterial hypertension and in vitro pulmonary hypertension models. In the in vivo model, male Sprague Dawley rats received a single subcutaneous injection of Sugen SU5416 (20 mg/kg) prior to two weeks of hypobaric hypoxia (380 mmHg) followed by three weeks normoxia (Sugen/hypoxic), then animals were either maintained for three weeks on control chow or one containing apoptosis signal-regulating kinase 1 inhibitor (100 mg/kg/day). Cardiovascular measurements were carried out. In the in vitro model, primary cultures of rat pulmonary artery fibroblasts and rat pulmonary artery smooth muscle cells were maintained in hypoxia (5% O2) and investigated for proliferation, migration and molecular signalling in the presence or absence of apoptosis signal-regulating kinase 1 inhibitor. Sugen/hypoxic animals displayed significant pulmonary arterial hypertension compared to normoxic controls at eight weeks. Apoptosis signal-regulating kinase 1 inhibitor decreased right ventricular systolic pressure to control levels and reduced muscularised vessels in lung tissue. Apoptosis signal-regulating kinase 1 inhibition was found to prevent hypoxia-induced proliferation, migration and cytokine release in rat pulmonary artery fibroblasts and also prevented rat pulmonary artery fibroblast-induced rat pulmonary artery smooth muscle cell migration and proliferation. Apoptosis signal-regulating kinase 1 inhibition reversed pulmonary arterial hypertension in the Sugen/hypoxic rat model. These effects may be a result of intrinsic changes in the signalling of adventitial fibroblast.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pulm Circ Year: 2020 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pulm Circ Year: 2020 Document type: Article Affiliation country: United kingdom